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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 325379생성일: 2026년 10월 27일

Trichloroisocyanuric Acid → Ethyl (2-formamido-5-chlorothiazol-4-yl)glyoxylate

https://huagongshe.com/reaction/325379

반응식

참여 물질

역할이름HCID투입량
반응물Trichloroisocyanuric AcidHCID 6909—
반응물Ethyl 2-(formylamino)-alpha-oxo-4-thiazoleacetateHCID 2733245—
반응물HCID 178473042HCID 178473042—
용매DimethylformamideHCID 6228—
생성물Ethyl (2-formamido-5-chlorothiazol-4-yl)glyoxylateHCID 14326717—

반응 조건

온도60 °C

반응 단계

A suspension of ethyl 2-(2-formylamino-1,3-thiazol-4-yl)glyoxylate, which can be represented as ethyl 2-(2formylimino-2,3-dihydro-1,3-thiazol-4-yl)glyoxylate, (6.9 g.) in dimethylformamide (40 ml.) was heated at 60° C. to produce a solution, and to the solution was dropwise added a solution of trichloroisocyanuric acid (2.8 g.) in dimethylformamide (10 ml.) over 15 minutes at the same temperature with stirring and then the mixture was further stirred for 1 hours at the same temperature. After the reaction, the reaction mixture was poured into ice-water (400 g.). The precipitates were collected by filtration, washed with water and then dried to give ethyl 2-(2-formylamino-5-chloro-1,3-thiazol-4-yl)glyoxylate, which can be represented as ethyl 2-(2-formylimino-5-chloro-2,3-dihydro-1,3-thiazol-4-yl)glyoxylate, (7.1 g.), mp. 151° to 153° C. The remaining filtrate was extracted with ethyl acetate, and the extract was washed with water and then dried over magnesium sulfate. The solvent was distilled off from the extract to give further the same object compound (0.75 g.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04440766
출처 데이터셋uspto-grants-1984_04
ORD IDord-95debc1b2d264f41ad032a21cea6022d
출처 메모uspto-grants-1984_04